ATE446953T1 - P2X7 RECEPTOR ANTAGONISTS AND THEIR USE - Google Patents
P2X7 RECEPTOR ANTAGONISTS AND THEIR USEInfo
- Publication number
- ATE446953T1 ATE446953T1 AT04735697T AT04735697T ATE446953T1 AT E446953 T1 ATE446953 T1 AT E446953T1 AT 04735697 T AT04735697 T AT 04735697T AT 04735697 T AT04735697 T AT 04735697T AT E446953 T1 ATE446953 T1 AT E446953T1
- Authority
- AT
- Austria
- Prior art keywords
- receptor antagonists
- antagonists
- receptor
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Quinoline Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0312609.1A GB0312609D0 (en) | 2003-06-02 | 2003-06-02 | Novel compounds |
SE0301700A SE0301700D0 (en) | 2003-06-02 | 2003-06-10 | Novel compounds |
PCT/SE2004/000836 WO2004106305A1 (en) | 2003-06-02 | 2004-06-01 | New p2x7 receptor antagonists and their use |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE446953T1 true ATE446953T1 (en) | 2009-11-15 |
Family
ID=38812906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT04735697T ATE446953T1 (en) | 2003-06-02 | 2004-06-01 | P2X7 RECEPTOR ANTAGONISTS AND THEIR USE |
Country Status (25)
Country | Link |
---|---|
US (2) | US7408065B2 (en) |
EP (1) | EP1633717B1 (en) |
JP (1) | JP4682128B2 (en) |
KR (1) | KR101244971B1 (en) |
CN (1) | CN1832925B (en) |
AR (1) | AR045691A1 (en) |
AT (1) | ATE446953T1 (en) |
AU (1) | AU2004242626B2 (en) |
BR (1) | BRPI0410933A (en) |
CA (1) | CA2526884C (en) |
CO (1) | CO5700720A2 (en) |
DE (1) | DE602004023840D1 (en) |
ES (1) | ES2333721T3 (en) |
GB (1) | GB0312609D0 (en) |
IS (1) | IS8190A (en) |
MX (1) | MXPA05012883A (en) |
NO (1) | NO20060001L (en) |
RU (1) | RU2347778C2 (en) |
SA (1) | SA04250155B1 (en) |
SE (1) | SE0301700D0 (en) |
TW (1) | TW200508214A (en) |
UA (1) | UA83659C2 (en) |
UY (1) | UY28342A1 (en) |
WO (1) | WO2004106305A1 (en) |
ZA (1) | ZA200509706B (en) |
Families Citing this family (56)
Publication number | Priority date | Publication date | Assignee | Title |
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GB0312609D0 (en) | 2003-06-02 | 2003-07-09 | Astrazeneca Ab | Novel compounds |
US7141596B2 (en) | 2003-10-08 | 2006-11-28 | Incyte Corporation | Inhibitors of proteins that bind phosphorylated molecules |
WO2006032851A1 (en) * | 2004-09-20 | 2006-03-30 | Biolipox Ab | Pyrazole compounds useful in the treatment of inflammation |
JP2008526840A (en) * | 2005-01-06 | 2008-07-24 | アストラゼネカ アクチボラグ | New compounds |
US7297700B2 (en) * | 2005-03-24 | 2007-11-20 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
WO2006110516A1 (en) * | 2005-04-11 | 2006-10-19 | Abbott Laboratories | Acylhydrazide p2x7 antagonists and uses thereof |
US20080312208A1 (en) * | 2005-07-13 | 2008-12-18 | Astrazeneca Ab | Pyridine Analogues |
CN101232890A (en) * | 2005-08-01 | 2008-07-30 | 芬诺密克斯公司 | Methods of preparing heterocyclic boronic acids and derivatives thereof |
US7547782B2 (en) | 2005-09-30 | 2009-06-16 | Bristol-Myers Squibb Company | Met kinase inhibitors |
TW200800911A (en) * | 2005-10-20 | 2008-01-01 | Biolipox Ab | Pyrazoles useful in the treatment of inflammation |
AU2006310367A1 (en) * | 2005-10-31 | 2007-05-10 | Biolipox Ab | Triazole compounds as lipoxygenase inhibitors |
TW200732320A (en) * | 2005-10-31 | 2007-09-01 | Biolipox Ab | Pyrazoles useful in the treatment of inflammation |
JP2009513692A (en) * | 2005-11-01 | 2009-04-02 | バイオリポックス エービー | Pyrazole compounds useful for the treatment of inflammation |
US8007849B2 (en) | 2005-12-14 | 2011-08-30 | International Flavors & Fragrances Inc. | Unsaturated cyclic and acyclic carbamates exhibiting taste and flavor enhancement effect in flavor compositions |
TWI464148B (en) | 2006-03-16 | 2014-12-11 | Evotec Us Inc | Bicycloheteroaryl compounds as p2x7 modulators and uses thereof |
ES2569677T3 (en) | 2006-03-16 | 2016-05-12 | Second Genome, Inc. | Bicycloheteroaryl compounds as modulators of P2X7 and uses thereof |
US20090298825A1 (en) * | 2006-03-16 | 2009-12-03 | Kelly Michael G | Bicycloheteroaryl Compounds as P2x7 Modulators and Uses Thereof |
EP1937643B1 (en) * | 2006-03-16 | 2016-07-13 | Second Genome, Inc. | Bicycloheteroaryl compounds as p2x7 modulators and uses thereof |
US20080058309A1 (en) * | 2006-07-27 | 2008-03-06 | Astrazeneca Ab | Novel Compounds 171 |
MX2009003170A (en) * | 2006-09-28 | 2009-04-03 | Hoffmann La Roche | Quinoline derivatives with 5-ht-binding properties. |
ZA200904477B (en) | 2006-11-27 | 2010-09-29 | Lundbeck & Co As H | Heteroaryl amide derivatives |
WO2008068157A1 (en) * | 2006-12-07 | 2008-06-12 | F. Hoffmann-La Roche Ag | 2-aminoquinolines as 5-ht(5a) receptor antagonists |
CA2680761A1 (en) | 2007-03-22 | 2008-09-25 | Astrazeneca Ab | Quinoline derivatives for the treatment of inflammatory diseases |
EP2592082A1 (en) * | 2007-04-10 | 2013-05-15 | H. Lundbeck A/S | Heteroaryl amide analogues as p2x7 antagonists |
PE20091036A1 (en) * | 2007-11-30 | 2009-08-15 | Astrazeneca Ab | QUINOLINE DERIVATIVE AS ANTAGONIST OF THE P2X7 RECEPTOR |
WO2009108551A2 (en) * | 2008-02-25 | 2009-09-03 | H. Lundbeck A/S | Heteroaryl amide analogues |
CA2715842A1 (en) | 2008-03-07 | 2009-09-11 | F. Hoffmann-La Roche Ag | 2-aminoquinoline derivatives |
ATE494926T1 (en) | 2008-03-25 | 2011-01-15 | Affectis Pharmaceuticals Ag | NOVEL P2X7R ANTAGONISTS AND THEIR USE |
AU2009239471B2 (en) * | 2008-04-22 | 2013-01-24 | Janssen Pharmaceutica Nv | Quinoline or isoquinoline substituted P2X7 antagonists |
ES2380908T3 (en) | 2009-04-14 | 2012-05-21 | Affectis Pharmaceuticals Ag | Novelty p2x7r antagonists and their use |
CA2761639C (en) * | 2009-05-29 | 2016-06-07 | Raqualia Pharma Inc. | Aryl substituted carboxamide derivatives as calcium or sodium channel blockers |
EP2386541A1 (en) | 2010-05-14 | 2011-11-16 | Affectis Pharmaceuticals AG | Novel methods for the preparation of P2X7R antagonists |
WO2012110190A1 (en) | 2011-02-17 | 2012-08-23 | Affectis Pharmaceuticals Ag | Novel p2x7r antagonists and their use |
WO2012163792A1 (en) | 2011-05-27 | 2012-12-06 | Affectis Pharmaceuticals Ag | Novel p2x7r antagonists and their use |
WO2012163456A1 (en) | 2011-05-27 | 2012-12-06 | Affectis Pharmaceuticals Ag | Novel p2x7r antagonists and their use |
CN103687860B (en) | 2011-07-22 | 2016-06-08 | 埃科特莱茵药品有限公司 | As P2X7The heterocyclic amide derivative of receptor antagonist |
CN104066737B (en) | 2012-01-20 | 2016-06-08 | 埃科特莱茵药品有限公司 | As P2X7The heterocyclic amide derivative of receptor antagonist |
US9718774B2 (en) | 2012-12-12 | 2017-08-01 | Idorsia Pharmaceuticals Ltd | Indole carboxamide derivatives as P2X7 receptor antagonist |
WO2014097140A1 (en) | 2012-12-18 | 2014-06-26 | Actelion Pharmaceuticals Ltd | Indole carboxamide derivatives as p2x7 receptor antagonists |
JP6282016B2 (en) | 2013-01-22 | 2018-02-21 | イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd | Heterocyclic amide derivatives as P2X7 receptor antagonists |
ES2616883T3 (en) | 2013-01-22 | 2017-06-14 | Actelion Pharmaceuticals Ltd. | Heterocyclic amide derivatives as P2X7 receptor antagonists |
US10053463B2 (en) | 2013-03-14 | 2018-08-21 | Janssen Pharmaceutica Nv | Substituted [1,2,4]triazolo[4,3-a]pyrazines as P2X7 modulators |
JO3773B1 (en) | 2013-03-14 | 2021-01-31 | Janssen Pharmaceutica Nv | P2X7 rates |
JO3509B1 (en) | 2013-03-14 | 2020-07-05 | Janssen Pharmaceutica Nv | P2x7 modulators |
WO2014152589A1 (en) | 2013-03-14 | 2014-09-25 | Janssen Pharmaceutica Nv | P2x7 modulators |
AR100724A1 (en) * | 2014-06-05 | 2016-10-26 | Merck Patent Gmbh | DERIVATIVES OF QUINOLINA AND ITS USE IN NEURODEGENERATIVE DISEASES |
US20180118749A1 (en) | 2014-09-12 | 2018-05-03 | Janssen Pharmaceutica Nv | P2x7 modulators |
AU2015315687B2 (en) | 2014-09-12 | 2019-07-11 | Janssen Pharmaceutica Nv | P2X7 modulators |
CN106084068B (en) * | 2016-06-16 | 2019-07-16 | 郑州大学第一附属医院 | A Group of Enterobactin-Antibiotic Derivatives and Their Applications |
RS64995B1 (en) * | 2017-03-13 | 2024-01-31 | Raqualia Pharma Inc | Tetrahydroquinoline derivatives as p2x7 receptor antagonists |
EP3398941A1 (en) * | 2017-05-03 | 2018-11-07 | AXXAM S.p.A. | Heterocyclic p2x7 antagonists |
US20200102311A1 (en) | 2018-09-28 | 2020-04-02 | Janssen Pharmaceutica Nv | Monoacylglycerol Lipase Modulators |
JOP20210058A1 (en) | 2018-09-28 | 2021-03-24 | Janssen Pharmaceutica Nv | Monoacylglycerol lipase modulators |
KR20220075386A (en) | 2019-09-30 | 2022-06-08 | 얀센 파마슈티카 엔.브이. | Radiolabeled MGL PET Ligand |
EP4126860A1 (en) | 2020-03-26 | 2023-02-08 | Janssen Pharmaceutica NV | Monoacylglycerol lipase modulators |
CN115305282A (en) * | 2022-08-04 | 2022-11-08 | 烟台毓璜顶医院 | A target and treatment method for AR-induced OD diagnosis and prognosis |
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US3471491A (en) * | 1967-08-28 | 1969-10-07 | Squibb & Sons Inc | Adamantyl-s-triazines |
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IL53441A0 (en) | 1977-11-22 | 1978-01-31 | Teva Pharma | Methyladamantyl hydrazines their preparation and pharmaceutical compositions containing them |
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GB0013737D0 (en) | 2000-06-07 | 2000-07-26 | Astrazeneca Ab | Novel compounds |
CN1261099C (en) * | 2001-07-02 | 2006-06-28 | 阿克佐诺贝尔公司 | Tetrahydroquinoline derivatives |
WO2003042190A1 (en) | 2001-11-12 | 2003-05-22 | Pfizer Products Inc. | N-alkyl-adamantyl derivatives as p2x7-receptor antagonists |
SE0103836D0 (en) * | 2001-11-16 | 2001-11-16 | Astrazeneca Ab | Novel compounds |
JP2005519876A (en) | 2001-11-27 | 2005-07-07 | メルク エンド カムパニー インコーポレーテッド | 2-aminoquinoline compounds |
SE0200920D0 (en) * | 2002-03-25 | 2002-03-25 | Astrazeneca Ab | Novel compounds |
GB0312609D0 (en) | 2003-06-02 | 2003-07-09 | Astrazeneca Ab | Novel compounds |
SE0302139D0 (en) | 2003-07-28 | 2003-07-28 | Astrazeneca Ab | Novel compounds |
SE0402925D0 (en) | 2004-11-30 | 2004-11-30 | Astrazeneca Ab | Novel Compounds |
-
2003
- 2003-06-02 GB GBGB0312609.1A patent/GB0312609D0/en not_active Ceased
- 2003-06-10 SE SE0301700A patent/SE0301700D0/en unknown
-
2004
- 2004-01-06 UA UAA200510608A patent/UA83659C2/en unknown
- 2004-05-27 TW TW093115168A patent/TW200508214A/en unknown
- 2004-06-01 RU RU2005136130/04A patent/RU2347778C2/en not_active IP Right Cessation
- 2004-06-01 CN CN2004800222482A patent/CN1832925B/en not_active Expired - Fee Related
- 2004-06-01 WO PCT/SE2004/000836 patent/WO2004106305A1/en active Application Filing
- 2004-06-01 AT AT04735697T patent/ATE446953T1/en not_active IP Right Cessation
- 2004-06-01 DE DE602004023840T patent/DE602004023840D1/en not_active Expired - Lifetime
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2005
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2006
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